JPH0270056A - Production of nitrided parts - Google Patents

Production of nitrided parts

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Publication number
JPH0270056A
JPH0270056A JP18727488A JP18727488A JPH0270056A JP H0270056 A JPH0270056 A JP H0270056A JP 18727488 A JP18727488 A JP 18727488A JP 18727488 A JP18727488 A JP 18727488A JP H0270056 A JPH0270056 A JP H0270056A
Authority
JP
Japan
Prior art keywords
comparative example
nitriding
parts
less
steel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP18727488A
Other languages
Japanese (ja)
Inventor
Tadaki Itabe
板部 忠喜
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Komatsu Ltd
Original Assignee
Komatsu Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Komatsu Ltd filed Critical Komatsu Ltd
Priority to JP18727488A priority Critical patent/JPH0270056A/en
Publication of JPH0270056A publication Critical patent/JPH0270056A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To efficiently produce nitrided part having high toughness by heating parts having a specified compsn. contg. C, Si, Mn, Cr, V, Al, P, S, Cu, Ni, Sn and Fe as essential components at a specified temp. and by rapidly cooling the heated parts. CONSTITUTION:A quick-nitriding steel consisting of 0.20-0.50% C, <=0.30% Si, 0.50-1.50% Mn, <=1.20% Cr, 0.05-0.30% V, 0.05-0.30% Al, <=0.02% each of P and S, <=0.05% each of Cu, Ni and Sn and the balance Fe with inevitable impurities or further contg. 0.10-0.40% Mo is heated at 800-900 deg.C and rapidly cooled. By using the steel, nitrided parts having high toughness are obtd. by short-time nitriding.

Description

【発明の詳細な説明】 (産業上の利用骨!!F) 本発明は、窒化部品の製造方法に関するもので、窒化処
理時間の短縮と窒化後の高い靭性を有する製造方法に関
する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Use!!F) The present invention relates to a method for manufacturing nitrided parts, and relates to a manufacturing method that shortens nitriding time and provides high toughness after nitriding.

(従来の技術) 機械構造用部品の窒化処理を短時間で行うために各種の
迅速窒化鋼が提唱されている。その中で窒化処理後にH
v20.0以上の芯部硬さが必要な場合には例えば特開
昭62−7243号公報等に開示される■添加型の迅速
窒化鋼が最も有効である。
(Prior Art) Various types of rapid nitriding steels have been proposed in order to perform nitriding treatment of mechanical structural parts in a short time. After nitriding treatment, H
When a core hardness of v20.0 or more is required, the most effective is the rapid nitriding steel of the type (3), which is disclosed in, for example, Japanese Unexamined Patent Publication No. 62-7243.

(発明が解決しようとする課題) しかし、上記の従来技術のものは迅速な窒化処理が可能
であるが、第2図の比較例B−1が示すように窒化処理
後靭性が低いという問題点がある。
(Problems to be Solved by the Invention) However, although the above-mentioned conventional technology allows rapid nitriding, it has the problem of low toughness after nitriding, as shown in Comparative Example B-1 in FIG. There is.

又、Ti添加によりTiN、Ticを析出しオーステナ
イト粒度の微細化やMn、、B等の添加により非調質状
態で靭性の高いベイナイト組織にする方法も試みられて
いるが第4図の比較例C−2に示す様に靭性(例えば衝
撃値)はほとんど改善されないという問題点がある。
In addition, attempts have been made to precipitate TiN and Tic by adding Ti to refine the austenite grain size, and to create a bainite structure with high toughness in a non-thermal condition by adding Mn, B, etc., but the comparative example shown in Fig. 4 As shown in C-2, there is a problem in that the toughness (for example, impact value) is hardly improved.

本発明かかる従来技術の問題点を解決するものである。The present invention solves the problems of the prior art.

(課題を解決するための手段及び作用)課題を解決する
ために (1)次の組成を必須成分として持ち、かつ800〜9
00℃で加熱後筒、冷することを特徴とする窒化部品の
製造方法とした。
(Means and effects for solving the problem) In order to solve the problem: (1) It has the following composition as an essential component, and 800 to 9
This method of manufacturing nitrided parts is characterized by heating the cylinder at 00°C and then cooling it.

C:0.20〜0.50% Si:0.30%以下 Mn : 0. 50〜1. 50% Cr:1.20%以下 :0.05〜0.30% AI:0.05〜0.30% P S:それぞれ0.02%以下 Cu、Ni  Sn:それぞれ0.05%以下残部:F
eとその他年可避な不純物 (2)前記(1)の必須成分に、さらに、Mo:0.1
0〜0.40%を含んだ迅速窒化鋼の製造方法とした。
C: 0.20-0.50% Si: 0.30% or less Mn: 0. 50-1. 50% Cr: 1.20% or less: 0.05 to 0.30% AI: 0.05 to 0.30% PS: 0.02% or less each Cu, Ni Sn: 0.05% or less each Remainder: F
e and other inevitable impurities (2) In addition to the essential components of (1) above, Mo: 0.1
A method for producing rapid nitriding steel containing 0 to 0.40%.

(実施例) ここに本発明者が鋭意研究の結果、■添加型迅速窒化鋼
の窒化後の衝撃値を改善するためには、V4C,の析出
形態の制御が重要であることを知見した。すなわちオー
ステナイト化後の冷却途中650℃前後でオーステナイ
トとフェライトの相界面に析出する■4C3が衝撃値を
低下させるものであると推定されるので、V a C3
の相界面析出を阻止するため先に出願した特願昭62−
160428号記載の迅速窒化鋼を用いて実施した。
(Example) As a result of intensive research, the inventors of the present invention have found that controlling the precipitation form of V4C is important in order to improve the impact value after nitriding of (1) addition type rapid nitriding steel. In other words, it is estimated that ■4C3, which precipitates at the phase interface between austenite and ferrite at around 650°C during cooling after austenitization, reduces the impact value, so V a C3
A patent application previously filed in 1982 to prevent the phase interface precipitation of
The experiment was carried out using the rapid nitriding steel described in No. 160428.

第1表は供試材の化学成分を示すもので、No、 1は
比較mAT:scM440H材である。No、 2 、
 No、 3はそれぞれ比較鋼B、Cで■添加型迅速窒
化鋼である。No、 4 、 No、 5はそ、れぞれ
実施鋼り、Eであり本発明者が発明した特願昭62−1
60428号記載の■添加型迅速窒化鋼である。
Table 1 shows the chemical components of the test materials, and No. 1 is the comparative mAT:scM440H material. No, 2,
Nos. 3 and 3 are comparative steels B and C, respectively, which are ■ additive type rapid nitriding steels. No. 4, No. 5, and No. 5 are the actual steel sheets E, respectively, and are patent applications filed in 1982-1 invented by the present inventor.
This is a rapid nitriding steel with ■ addition type described in No. 60428.

第2表は第1表に示す供試材を前処理を表に示す条件で
行ったもので、窒化条件は570℃で4時間ガス軟窒化
後油冷を行ったものである。表中の[表面より0.05
mm部の硬さ」はビッカース硬変針で測定した結果であ
り、「硬化深さ」はHv400以上の硬さを示す部分の
深さである。「芯部硬さ」は中心部の硬さをビッカース
硬度計で測定した結果であり、「シャルピー衝撃値jは
2 mmのvノツチシャルピー試験片に全面に窒化処理
を行い20℃で試験を行った結果である。図中記号は第
1図〜第4図のグラフ中に用いられる記号を示すもので
ある。
In Table 2, the test materials shown in Table 1 were pretreated under the conditions shown in the table, and the nitriding conditions were gas nitrocarburizing at 570° C. for 4 hours followed by oil cooling. In the table [0.05 from the surface
"Hardness in mm section" is the result of measurement with a Vickers hardening needle, and "curing depth" is the depth of the part showing hardness of Hv400 or more. "Core hardness" is the result of measuring the hardness of the center using a Vickers hardness tester, and "Charpy impact value J" is the result of measuring the hardness of the center using a Vickers hardness tester. The symbols in the figure indicate the symbols used in the graphs of FIGS. 1 to 4.

第1図はシャルピー衝撃試験片の硬さ分布を示すグラフ
で、■添加の鋼に窒化した実施例1.実施例2.比較例
B−1は■が添加してない鋼に窒素した比較例A−1よ
りも硬化深さが深いことを示している。
Figure 1 is a graph showing the hardness distribution of Charpy impact test specimens, and shows Example 1. Example 2. Comparative Example B-1 shows that the hardening depth is deeper than Comparative Example A-1, in which nitrogen was added to steel without ■.

第2図は比較例B−1と実施例゛1.実施例2のシャル
ピー衝撃値の比較グラフであり、実施例1実施例2で示
す本発明のものが高い衝撃値を示している。第3図は比
較例A−1と比較例B−1のシャルピー衝撃値の比較で
あり、比較例A−1のシャルピー衝撃値は比較例B−]
よりも高いことを示すが比較例A−1は第1図に示す様
に■が添加されていないため窒化による硬化深が■添加
の鋼より浅くなっている。
FIG. 2 shows Comparative Example B-1 and Example 1. It is a comparison graph of the Charpy impact values of Example 2, and the one of the present invention shown in Example 1 and Example 2 shows a high impact value. Figure 3 is a comparison of the Charpy impact values of Comparative Example A-1 and Comparative Example B-1, and the Charpy impact value of Comparative Example A-1 is the same as that of Comparative Example B-]
However, as shown in FIG. 1, Comparative Example A-1 does not contain ``■'', so the hardening depth due to nitriding is shallower than that of the steel with ``■''.

第4図は比較例A−2と比較例B−2.比較例C1、比
較例C−2のシャルピー衝撃値の比較でありVが添加さ
れていない比較例A−2のシャルピーは衝撃値は■が添
加されている比較例B−2比較例C−L、比較例(、−
2より高いことを示すが■が添加されていないため窒化
による硬化深さが浅いのは前記と同様である。
FIG. 4 shows Comparative Example A-2 and Comparative Example B-2. This is a comparison of the Charpy impact values of Comparative Example C1 and Comparative Example C-2, and the Charpy of Comparative Example A-2 in which V is not added has an impact value of Comparative Example B-2 in which ■ is added.Comparative Example C-L , Comparative example (, -
Although it shows that the value is higher than 2, the hardening depth due to nitriding is shallow because ▪ is not added, as described above.

(発明の効果) 本発明の特許請求の範囲(1)のものによれば従来技術
のものに比べて、優れた靭性を得ることができる。
(Effects of the Invention) According to the invention set forth in claim (1), superior toughness can be obtained compared to those of the prior art.

特許請求の範囲(2)のものによれば特許請求の範囲(
1)のものより更に優れた靭性を得ることができる。
According to claim (2), the claim (
Even better toughness than 1) can be obtained.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はシャルピー衝撃試験片の硬さ分布、第2図は比
較例B−1と実施例1.実施例2のシャルピー衝撃値の
比較グラフ。 第3図は比較例A−1と比較例B−1のシャルピー衝撃
値の比較グラフ、第4図は比較例A−2と比較例B−2
,C−1,(、−2のシャルピー衝撃値の比較グラフを
それぞれ示す図である。
Fig. 1 shows the hardness distribution of the Charpy impact test specimens, and Fig. 2 shows the hardness distribution of the Charpy impact test pieces. A comparison graph of Charpy impact values of Example 2. Figure 3 is a comparison graph of Charpy impact values of Comparative Example A-1 and Comparative Example B-1, and Figure 4 is a graph of Comparative Example A-2 and Comparative Example B-2.
, C-1, (, -2) are graphs showing a comparison of Charpy impact values.

Claims (2)

【特許請求の範囲】[Claims] (1)次の組成を必須成分として持ち、かつ800〜9
00℃で加熱後急冷することを特徴とする窒化部品の製
造方法。 C:0.20〜0.50% Si:0.30%以下 Mn:0.50〜1.50% Cr:1.20%以下 V:0.05〜0.30% Al:0.05〜0.30% P、S:それぞれ0.02%以下 Cu、Ni、Sn:それぞれ0.05%以下残部:Fe
とその他不可避不純物
(1) Have the following composition as an essential component, and 800 to 9
A method for manufacturing nitrided parts, characterized by heating at 00°C and then rapidly cooling. C: 0.20~0.50% Si: 0.30% or less Mn: 0.50~1.50% Cr: 1.20% or less V: 0.05~0.30% Al: 0.05~ 0.30% P, S: 0.02% or less each Cu, Ni, Sn: 0.05% or less each Balance: Fe
and other unavoidable impurities
(2)必須成分に、さらに、 Mo:0.10〜0.40%を含んだ特許請求の範囲第
1項記載の迅速窒化鋼の製造方法。
(2) The method for producing rapid nitriding steel according to claim 1, wherein the essential components further include Mo: 0.10 to 0.40%.
JP18727488A 1988-07-26 1988-07-26 Production of nitrided parts Pending JPH0270056A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18727488A JPH0270056A (en) 1988-07-26 1988-07-26 Production of nitrided parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18727488A JPH0270056A (en) 1988-07-26 1988-07-26 Production of nitrided parts

Publications (1)

Publication Number Publication Date
JPH0270056A true JPH0270056A (en) 1990-03-08

Family

ID=16203126

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18727488A Pending JPH0270056A (en) 1988-07-26 1988-07-26 Production of nitrided parts

Country Status (1)

Country Link
JP (1) JPH0270056A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2811079A1 (en) 2013-06-03 2014-12-10 Kobelco Construction Machinery Co., Ltd. Construction machine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2811079A1 (en) 2013-06-03 2014-12-10 Kobelco Construction Machinery Co., Ltd. Construction machine

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